VOLUME VENTILATOR CIRCUIT W/WATER TRAP— 510(k) K834570

Name: FDA 510(k) clearance K834570
Creator: U.S. Food and Drug Administration
Published: 1984-03-05

Substantially Equivalent

Airlife, Inc.

FDA 510(k) clearance K834570 for VOLUME VENTILATOR CIRCUIT W/WATER TRAP, Substantially Equivalent on 1984-03-05. Applicant: Airlife, Inc.. Device class: 1.

Clearance details

Applicant: Airlife, Inc.
Product code: Code BZO
Device class: Class 1
Regulation: 21 CFR 868.5975
Advisory panel: Anesthesiology
Date received: 1983-12-29
Decision date: 1984-03-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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K832725 — DUAL DIAL VENTURI STYLE MASK1983-09-20

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